Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Beijing, Beijing Municipality, 100021, China
NCT Number: NCT06198907
This is a phase 2 Study to investigate the safety, tolerability, and anti-tumor activity of golidocitinib in combination with sintilimab as the front-line treatment for patients with metastatic PD-L1 positive non-small cell lung cancer (NSCLC)
Trial opening soon.
Get Notified18 year–75 year
All sexes
Interventional
Phase 2
Beijing, Beijing Municipality, 100021, China
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Part A Dose escalation:
Patients must have relapsed after or been refractory/intolerant to ≥ 1 prior systemic therapy(ies) for NSCLC
Part B dose expansion:
Exclusion criteria
Part A Dose escalation:
Part B Dose Expansion:
Daily dosing of golidocitinib
Sintilimab, 200mg, intravenous, every 3 weeks.
Pemetrexed or nab-paclitaxel +carboplatin, intravenous, every 3 weeks for 2 cycles
Time frame: through study completion, an average of 1 year
Complete response (CR) or partial response (PR) per investigator assessment according to RECIST 1.1
Time frame: through study completion, an average of 1 year
Time from first administration of study drug to first documented disease progression or death per investigator assessment according to RECIST 1.1
Time frame: through study completion, up to 36 months
time from first administration of study drug to death
Time frame: through study completion, up to 36 months
Frequency an severity of AEs according to the Common Terminology Criteria for Adverse Events (CTCAE) version 5.0.
Contact information is provided by the study sponsor or research team.
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Other
A Phase 2, Open-label, Single Arm Study to Investigate the Safety and Efficiency of Golidocitinib in Combination With Sintilimab in Patients With Locally Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC) With PD-L1TPS ≥ 1%)
Acronym: JACKPOT33
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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